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topspin nmr data analysis software  (Bruker Corporation)


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    Bruker Corporation topspin nmr data analysis software
    Topspin Nmr Data Analysis Software, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 14296 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nmr+software/TopSpin+Software/us12594308-632-9-8
    Average 99 stars, based on 14296 article reviews
    topspin nmr data analysis software - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Nuclear Magnetic Resonance:

    Article Title: Novel approach on the evaluation of enzyme-aided alkaline extraction of polysaccharide from Hordeum vulgare husk and molecular insight on the multifunctional scaffold.
    Article Snippet: Hordeum vulgare husk, a cereal grain, is rich in dietary fiber and prebiotics beneficial for the gut microbiota and host organism.. This study investigates the effects of barley husk-derived water-soluble xylan (BH-WSX) on gut homeostasis and the microbiome.. We enzymatically extracted BH-WSX and evaluated its prebiotic and antioxidant properties.

    Article Title: Unveiling Dissolution Kinetics of CuO Nanofertilizer Using Bio-Based Ionic Liquids Envisaging Controlled Use Efficiency for Sustainable Agriculture
    Article Snippet: .. Solutions containing [Cho][Asc] were evaluated by 1H NMR after 7 days, with the water peak suppressed by Bruker NMR software. .. Solutions containing [Cho][Asc] were evaluated by 1H NMR after 7 days, with the water peak suppressed by Bruker NMR software.

    Article Title: Versatile approach towards fully desymmetrized trehalose with a novel set of orthogonal protecting groups
    Article Snippet: .. NMR spectra were recorded on a Bruker Avance III 600 spectrometer ( 1 H at 600.22 MHz; 13 C at 150.93 MHz; 31 P at 242.97 MHz) using standard Bruker NMR software. ..

    Article Title: Expression and Characterisation of the First Snail-Derived UDP-Gal: Glycoprotein-N-acetylgalactosamine β-1,3-Galactosyltransferase (T-Synthase) from Biomphalaria glabrata .
    Article Snippet: Spectra were processed with the manufacturer’s software (Bruker Flexanalysis 3.3.80). .. NMR spectra were recorded with a Bruker Avance III 600 instrument (600.22 MHz for 1H, 150.93 MHz for 13C) using standard Bruker NMR software. ..

    Article Title: Exploring Species-Specificity in TLR4/MD-2 Inhibition with Amphiphilic Lipid A Mimicking Glycolipids.
    Article Snippet: Size exclusion chromatography was performed using Bio-Beads S-X1 support (BioRad, Darmstadt, Germany). .. NMR spectra were recorded on a Bruker Avance III 600 spectrometer (1H at 600.22 MHz; 13C at 150.93 MHz; 31P at 242.97 MHz) using standard Bruker NMR software. ..

    Article Title: A highly branched glucomannan from the fruiting body of Schizophyllum commune: Structural characteristics and antitumor properties analysis.
    Article Snippet: In this study, a highly branched glucomannan (SCP-1) from Schizophyllum commune fruiting body with good solubility was isolated, and its structural characteristics and antitumor properties were analyzed.. The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mannose with a relative molar ratio of 14:6:210:593:177, and the molecular weight (Mw) of SCP-1 was 15.1 kDa.. SCP-1 showed a rough and dense surface, and it was aggregated to particles in distilled water, though it might have triple-helix conformation.

    Article Title: A simple approach to produce hydrophobic biobased coatings using methylcellulose and organosolv lignin.
    Article Snippet: .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled. .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled.

    Software:

    Article Title: Novel approach on the evaluation of enzyme-aided alkaline extraction of polysaccharide from Hordeum vulgare husk and molecular insight on the multifunctional scaffold.
    Article Snippet: Hordeum vulgare husk, a cereal grain, is rich in dietary fiber and prebiotics beneficial for the gut microbiota and host organism.. This study investigates the effects of barley husk-derived water-soluble xylan (BH-WSX) on gut homeostasis and the microbiome.. We enzymatically extracted BH-WSX and evaluated its prebiotic and antioxidant properties.

    Article Title: Unveiling Dissolution Kinetics of CuO Nanofertilizer Using Bio-Based Ionic Liquids Envisaging Controlled Use Efficiency for Sustainable Agriculture
    Article Snippet: .. Solutions containing [Cho][Asc] were evaluated by 1H NMR after 7 days, with the water peak suppressed by Bruker NMR software. .. Solutions containing [Cho][Asc] were evaluated by 1H NMR after 7 days, with the water peak suppressed by Bruker NMR software.

    Article Title: COVID-19: A complex disease with a unique metabolic signature
    Article Snippet: .. To this aim, each spectrum was segmented into 0.02 ppm chemical shift bins, from 10.00 to 0.2 ppm, with the exclusion of EDTA resonances (regions: 2.53–2.60, 2.68–2.73, 3.07–3.24, 3.58–3.64 ppm) and water signal (region: 4.40–5.00 ppm); the corresponding spectral areas were integrated (Assure-NMR software, Bruker BioSpin). ..

    Article Title: Versatile approach towards fully desymmetrized trehalose with a novel set of orthogonal protecting groups
    Article Snippet: .. NMR spectra were recorded on a Bruker Avance III 600 spectrometer ( 1 H at 600.22 MHz; 13 C at 150.93 MHz; 31 P at 242.97 MHz) using standard Bruker NMR software. ..

    Article Title: Expression and Characterisation of the First Snail-Derived UDP-Gal: Glycoprotein-N-acetylgalactosamine β-1,3-Galactosyltransferase (T-Synthase) from Biomphalaria glabrata .
    Article Snippet: Spectra were processed with the manufacturer’s software (Bruker Flexanalysis 3.3.80). .. NMR spectra were recorded with a Bruker Avance III 600 instrument (600.22 MHz for 1H, 150.93 MHz for 13C) using standard Bruker NMR software. ..

    Article Title: Exploring Species-Specificity in TLR4/MD-2 Inhibition with Amphiphilic Lipid A Mimicking Glycolipids.
    Article Snippet: Size exclusion chromatography was performed using Bio-Beads S-X1 support (BioRad, Darmstadt, Germany). .. NMR spectra were recorded on a Bruker Avance III 600 spectrometer (1H at 600.22 MHz; 13C at 150.93 MHz; 31P at 242.97 MHz) using standard Bruker NMR software. ..

    Article Title: A highly branched glucomannan from the fruiting body of Schizophyllum commune: Structural characteristics and antitumor properties analysis.
    Article Snippet: In this study, a highly branched glucomannan (SCP-1) from Schizophyllum commune fruiting body with good solubility was isolated, and its structural characteristics and antitumor properties were analyzed.. The monosaccharides of SCP-1 were fucose, glucosamine hydrochloride, galactose, glucose and mannose with a relative molar ratio of 14:6:210:593:177, and the molecular weight (Mw) of SCP-1 was 15.1 kDa.. SCP-1 showed a rough and dense surface, and it was aggregated to particles in distilled water, though it might have triple-helix conformation.

    Article Title: A simple approach to produce hydrophobic biobased coatings using methylcellulose and organosolv lignin.
    Article Snippet: .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled. .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled.

    Functional Assay:

    Article Title: A simple approach to produce hydrophobic biobased coatings using methylcellulose and organosolv lignin.
    Article Snippet: .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled. .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled.

    Labeling:

    Article Title: A simple approach to produce hydrophobic biobased coatings using methylcellulose and organosolv lignin.
    Article Snippet: .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled. .. The 2D HSQC NMR spectra, which can identify many more functional groups of the organosolv lignin, are shown in Fig. S2 (ESI†), with the full data from the NMR software (Bruker TopSpin) provided as ESI.† An important feature of different types of lignin is the syringyl to guaiacyl (S/G) ratios, which can be accurately determined using the 2D HSQC NMR spectra.49 Fig. 1 presents a section of the 2D HSQC NMR spectra of the organosolv lignin, with the blue contours indicating the peaks in the spectra, and the S2/6 and G2 contours labeled.



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    Glucose metabolism is the main pathway for aryl hydrocarbon receptor (AhR) activation to down-regulate the neutrophil elastase (NE) activity. (a) The diagram of glucose metabolism. (b-e) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of lipopolysaccharide (LPS, 10 μg/mL) or phorbol-12-myristate-13-acetate (PMA, 50 nM). The levels of Magt1, Magt 2, Magt 4, Magt5 and glutamine-fructose-6-phosphate transaminase (GFPT) were detected. (f-j) The neutrophils were treated with FICZ (100 nM) at the present or absence of LPS (10 μg/mL), and the intracellular metabolites were detected using a high-resolution <t>nuclear</t> <t>magnetic</t> resonance <t>(NMR).</t> The results were analyzed by PCA (f) , PLS (g) , OPLS (h) , KEGG enrichment analysis (i) and cluster analysis (j) . (k, l) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM). The relative glucose uptake (k) and intracellular pH values (l) were determined. (m, n) The neutrophils were treated with FICZ (100 nM) or DIM (10 μM) alone or in combination with L-sodium lactate (20 mM), ATP (100 μM) or GlcNAc (20 mM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM), and the release of dsDNA (m) and NE activity (n) was determined. The data were presented as the means ± S.E.M. of three or five independent experiments. ## p < 0.01 vs. Control group; * p < 0.05, ** p < 0.01 vs. LPS group; $$ p < 0.01 vs. LPS + FICZ group; ++ p < 0.01 vs. LPS + DIM group.
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    Image Search Results


    Glucose metabolism is the main pathway for aryl hydrocarbon receptor (AhR) activation to down-regulate the neutrophil elastase (NE) activity. (a) The diagram of glucose metabolism. (b-e) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of lipopolysaccharide (LPS, 10 μg/mL) or phorbol-12-myristate-13-acetate (PMA, 50 nM). The levels of Magt1, Magt 2, Magt 4, Magt5 and glutamine-fructose-6-phosphate transaminase (GFPT) were detected. (f-j) The neutrophils were treated with FICZ (100 nM) at the present or absence of LPS (10 μg/mL), and the intracellular metabolites were detected using a high-resolution nuclear magnetic resonance (NMR). The results were analyzed by PCA (f) , PLS (g) , OPLS (h) , KEGG enrichment analysis (i) and cluster analysis (j) . (k, l) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM). The relative glucose uptake (k) and intracellular pH values (l) were determined. (m, n) The neutrophils were treated with FICZ (100 nM) or DIM (10 μM) alone or in combination with L-sodium lactate (20 mM), ATP (100 μM) or GlcNAc (20 mM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM), and the release of dsDNA (m) and NE activity (n) was determined. The data were presented as the means ± S.E.M. of three or five independent experiments. ## p < 0.01 vs. Control group; * p < 0.05, ** p < 0.01 vs. LPS group; $$ p < 0.01 vs. LPS + FICZ group; ++ p < 0.01 vs. LPS + DIM group.

    Journal: Journal of Advanced Research

    Article Title: Aryl hydrocarbon receptor impairs HK2-controlled flux of the hexosamine biosynthesis pathway to suppress NETosis in an N -glycosylation-dependent manner

    doi: 10.1016/j.jare.2025.06.078

    Figure Lengend Snippet: Glucose metabolism is the main pathway for aryl hydrocarbon receptor (AhR) activation to down-regulate the neutrophil elastase (NE) activity. (a) The diagram of glucose metabolism. (b-e) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of lipopolysaccharide (LPS, 10 μg/mL) or phorbol-12-myristate-13-acetate (PMA, 50 nM). The levels of Magt1, Magt 2, Magt 4, Magt5 and glutamine-fructose-6-phosphate transaminase (GFPT) were detected. (f-j) The neutrophils were treated with FICZ (100 nM) at the present or absence of LPS (10 μg/mL), and the intracellular metabolites were detected using a high-resolution nuclear magnetic resonance (NMR). The results were analyzed by PCA (f) , PLS (g) , OPLS (h) , KEGG enrichment analysis (i) and cluster analysis (j) . (k, l) The neutrophils were treated with FICZ (100 nM), DIM (10 μM) or CH223191 (10 μM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM). The relative glucose uptake (k) and intracellular pH values (l) were determined. (m, n) The neutrophils were treated with FICZ (100 nM) or DIM (10 μM) alone or in combination with L-sodium lactate (20 mM), ATP (100 μM) or GlcNAc (20 mM) at the present or absence of LPS (10 μg/mL) or PMA (50 nM), and the release of dsDNA (m) and NE activity (n) was determined. The data were presented as the means ± S.E.M. of three or five independent experiments. ## p < 0.01 vs. Control group; * p < 0.05, ** p < 0.01 vs. LPS group; $$ p < 0.01 vs. LPS + FICZ group; ++ p < 0.01 vs. LPS + DIM group.

    Article Snippet: The collected nuclear magnetic resonance (NMR) spectra were analysed using Chenomx NMR Suite software, and statistical analysis with data visualisation was performed using the MetaboAnalyst platform.

    Techniques: Activation Assay, Activity Assay, Nuclear Magnetic Resonance, Control